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21740-00-1

21740-00-1 Structure

21740-00-1 Structure
IdentificationMore
[Name]

5-Bromo-2-iodobenzoic acid
[CAS]

21740-00-1
[Synonyms]

5-BROMO-2-IODOBENZOIC ACID
RARECHEM AL BO 0892
[EINECS(EC#)]

675-666-4
[Molecular Formula]

C7H4BrIO2
[MDL Number]

MFCD00079717
[Molecular Weight]

326.91
[MOL File]

21740-00-1.mol
Chemical PropertiesBack Directory
[Melting point ]

161-163°C
[Boiling point ]

133-134 °C(Press: 1 Torr)
[density ]

2.331±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[solubility ]

soluble in Methanol
[form ]

Solid
[pka]

2.47±0.10(Predicted)
[color ]

White to Light yellow
[Water Solubility ]

Slightly soluble in water.
[Sensitive ]

Light Sensitive
[InChI]

InChI=1S/C7H4BrIO2/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3H,(H,10,11)
[InChIKey]

IGBNDUKRHPTOBP-UHFFFAOYSA-N
[SMILES]

C(O)(=O)C1=CC(Br)=CC=C1I
[CAS DataBase Reference]

21740-00-1(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[HS Code ]

29163990
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Chemical Properties]

off-white light yellow powder
[Uses]

It is an important raw material and intermediate used in organic synthesis agrochemical, pharmaceutical and dyestuff field.
[Synthesis]

2-Amino-5-bromobenzoic acid

5794-88-7

5-Bromo-2-iodobenzoic acid

21740-00-1

General procedure for the synthesis of 5-bromo-2-iodobenzoic acid from 2-amino-5-bromobenzoic acid: a solution of 2-amino-5-bromobenzoic acid (3.9 g, 0.018 mol), sodium nitrite (NaNO2, 1.5 g, 0.022 mol) and sodium hydroxide (NaOH, 0.90 g, 0.023 mmol) in water (55 mL) was added dropwise to a stirred of a concentrated hydrochloric acid solution. The hydrochloric acid (HCl, 6.4 mL) in water (9 mL) solution was cooled at 0°C for 1.5 hours. After dropwise addition, stirring was continued for 30 minutes at 0°C. The formed diazonium salt suspension was added to a stirred solution of potassium iodide (KI, 4.5 g, 0.027 mol) and concentrated hydrochloric acid. A solution of sulfuric acid (H2SO4, 1.1 mL) in water (7.4 mL) was slowly added over 20 minutes at 35 to 40°C. The mixture was then heated to 90 °C and stirred for 30 min. Unreacted iodine was removed by steam distillation. The mixture was stirred and cooled. The crude product was filtered and washed with cold water, then dissolved in 40% aqueous sodium hydroxide. The polymer fraction was separated by decantation and the clarified solution was acidified with concentrated hydrochloric acid. The product was extracted with ether (Et2O). The extract was dried with anhydrous magnesium sulfate (MgSO4) and concentrated in vacuum. The residue was crystallized from a solvent mixture of methanol (MeOH) and water (H2O) (1:1, v/v) to give 5-bromo-2-iodobenzoic acid (3.56 g, 0.0109 mol, 60% yield) as a light yellow solid.

[References]

[1] Angewandte Chemie - International Edition, 2011, vol. 50, # 46, p. 10851 - 10854
[2] Organic Letters, 2008, vol. 10, # 14, p. 3001 - 3004
[3] Tetrahedron, 2011, vol. 67, # 1, p. 125 - 143
[4] Angewandte Chemie - International Edition, 2012, vol. 51, # 12, p. 2925 - 2929
[5] Collection of Czechoslovak Chemical Communications, 1984, vol. 49, # 1, p. 86 - 109
Spectrum DetailBack Directory
[Spectrum Detail]

5-Bromo-2-iodobenzoic acid(21740-00-1)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

21740-00-1(sigmaaldrich)
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